Canonical Allele Identifier: CA2804714152
Gene: HCN4 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73323143_73323144insT , CM000677.2:g.73323143_73323144insT GRCh38
NC_000015.9:g.73615484_73615485insT , CM000677.1:g.73615484_73615485insT GRCh37
NC_000015.8:g.71402537_71402538insT NCBI36
NG_009063.1:g.51121_51122insA

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.2949_2950insA MANE Select ENSP00000261917.3:p.Leu984ThrfsTer19
ENST00000261917.3:c.2949_2950insA ENSP00000261917.3:p.Leu984ThrfsTer19
NM_005477.2:c.2949_2950insA NP_005468.1:p.Leu984ThrfsTer19
XM_011521148.1:c.1731_1732insA XP_011519450.1:p.Leu578ThrfsTer19
XM_011521148.2:c.1731_1732insA XP_011519450.1:p.Leu578ThrfsTer19
NM_005477.3:c.2949_2950insA MANE Select NP_005468.1:p.Leu984ThrfsTer19
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